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Clinical Research Trials Coordinator Jobs in Missouri

Clinical Trials Data Coordinator - Remote
By City of Hope At California, United States
Basic education, experience and skills required for consideration:
Data Management & Protocol Compliance
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
Project Manager - Clinical Trials Office (Remote)
By City of Hope At California, United States
Minimum of 2 years of experience related to the regulatory management and conduct of oncology clinical trials in an academic setting.
Excellent skills in time management, prioritization, and multi-tasking required.
Basic education, experience, and skills required for consideration:
Must have working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.
Demonstrate strong organizational skills and ability to practice independently.
PM will exhibit expertise in the regulatory and operations arena of clinical trials.
Clinical Research Coordinator Jobs
By University of Missouri - Kansas City At , Kansas City, 64110, Mo $50,367 - $91,392 a year
Know Your Rights English Version
Know Your Rights Spanish Version
Salary Range: $50,367 - $91,392
Internal applicants can determine their university title by accessing the Talent Profile tile in myHR.
8:00 a.m. – 5:00 p.m.
Some weeknights or weekends necessary to ensure proper enrollment for clinic trials.
Clinical Trials Data Coordinator (Remote)
By City of Hope At California, United States
Basic education, experience, and skills required for consideration:
Preferred education, experience, and skills:
City of Hope’s commitment to Diversity, Equity, and Inclusion
Clinical Research Coordinator Jobs
By The IMA Group At St Louis, MO, United States
Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.
Additional duties and responsibilities may be assigned as needed.
Strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
Clinical Research Coordinator - Remote
By City of Hope At California, United States
Bachelor’s Degree. Experience may substitute for minimum education requirements. (i.e. Associate Degree plus two years of experience.)
Basic education, experience and skills required for consideration:
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
Assist the Epic Protocol Content Administrators (PCAs) with questions regarding the protocol procedural requirements, including lab tests, EKG’s or imaging.

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are looking for a Clinical Research Trials Coordinator to join our team and help us develop and execute clinical trials for our cutting-edge medical products. As a Clinical Research Trials Coordinator, you will be responsible for coordinating all aspects of clinical trials, from protocol development to data collection and analysis. You will also be responsible for ensuring compliance with all applicable regulations and guidelines. If you are a detail-oriented professional with a passion for clinical research, this is the perfect job for you!

Overview:

A Clinical Research Trials Coordinator is responsible for coordinating and managing clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations.

Detailed Job Description:

Clinical Research Trials Coordinators are responsible for the planning, implementation, and management of clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations. They must also coordinate with other members of the research team, such as physicians, nurses, and other healthcare professionals. Clinical Research Trials Coordinators must be able to effectively communicate with participants and other members of the research team. They must also be able to interpret and analyze data, and provide feedback to the research team.

What is Clinical Research Trials Coordinator Job Skills Required?

• Excellent communication and interpersonal skills
• Strong organizational and time management skills
• Ability to interpret and analyze data
• Knowledge of applicable regulations and guidelines
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

What is Clinical Research Trials Coordinator Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (optional)

What is Clinical Research Trials Coordinator Job Knowledge?

• Knowledge of clinical research protocols and procedures
• Knowledge of applicable regulations and guidelines
• Knowledge of data collection and analysis
• Knowledge of medical terminology

What is Clinical Research Trials Coordinator Job Experience?

• Experience in clinical research
• Experience in data collection and analysis
• Experience in recruiting and enrolling participants

What is Clinical Research Trials Coordinator Job Responsibilities?

• Recruit and enroll participants for clinical research trials
• Collect and manage data for clinical research trials
• Ensure compliance with all applicable regulations and guidelines
• Coordinate with other members of the research team
• Interpret and analyze data
• Provide feedback to the research team